Manufacture of composite ferrites

ABSTRACT

Ferrite powder of consistent good quality and homogeneity is obtained by using nitric acid to form solutions of the nitrate of each of the metals involved, mixing the solutions in the requisite proportions, and decomposing the mixture by deposition on a hot surface while avoiding any accumulation of liquid, and then calcining the obtained oxide mixture to obtain ferrite powder with a desired proportion of ready-formed ferrite. The nitrous gases formed during solution and decomposition are used for the reconstitution of nitric acid, the tail gas of the reconstitution system being preferably contacted with an aqueous suspension of a basic oxide of a constituent metal of the ferrite, thereby forming the nitrate solution of the constituent metal.

United States Patent Cowlard et al.

MANUFACTURE OF COMPOSITE FERRITES Frederick C. Cowlard; George 0rd, both of llford, England Inventors:

Assignee: The Plessy Company Limited, llford, En

gland Filed: Nov. 12, 1970 Appl. No.: 89,013

Related US. Application Data Continuation of Ser. No. 719,878, Apr. 9, 1968, abandoned.

US. Cl ..23/51, 252/6256, 252/6262, 252/6263 Int. Cl. ..C01g 49/00, C04b 35/26 Field of Search ..252/62.56-62.64; 23/51 5] Feb. 29, 1972 [56] References Cited UNITED STATES PATENTS 3,305,349 2/1967 Bovarnick ..75/.5 3,378,335 4/l968 Ellis et al. ..252/62.56

Primary ExaminerRobert D. Edmonds Attorney-Blum, Moscovitz, Friedman & Kaplan [5 7] ABSTRACT Ferrite powder of consistent good quality and homogeneity is obtained by using nitric acid to form solutions of the nitrate of 3 Claims, 1 Drawing Figure MANUFACTURE OF COMPOSITE FERRITES This application is a continuation of our copending application Ser. No. 719,878, which was filed Apr. 9, 1968, now abandoned for Manufacture of Composite Ferrites.

This invention relates to the manufacture of composite ferrites and has for an object to provide an improved process for the production of composite ferrites to fairly accurate specifications and with a good degree of homogeneity.

The process hitherto most widely employed to obtain composite ferrites uses as starting materials oxides or carbonates of each of the various metals intended to be present in the ferrite, these oxides or carbonates being ground to a fine powder and mechanically mixed to obtain a mixed powder in which the individual particles of each are as uniformly as possible distributed; this mixed powder was then calcined to cause the carbonates to decompose to oxides and a desired proportion of the oxides to react to form ferrites, an operation which involves sintering, the product thus obtained is pulverized again to obtain a moulding material for bodies of desired shape, and the bodies are then finally sintered to complete the reaction and obtain the desired ferrite bodies.

It is, however, difficult to obtain oxides free from alkali metals, and apart from the relatively high cost of oxides of the requisite degree of purity, the method involves considerable uncertainty due to variation from batch to batch of the purity, grain size, etc., of the purchased oxides. In order to reduce these last-mentioned difficulties, it has been proposed to obtain the required oxide mixture by other means, for example by electrolytic coprecipitation of the various metal oxide or chemical coprecipitation as oxalates. The last-mentioned process is, however limited to batch operation and gelatinous precipitates are formed which again are difficult to purify and filter.

The present invention proposes to produce powder of a ferrite containing a plurality of metal by the steps of heat decomposition of a mixed aqueous solution of nitrates of the various metals to be present in the ferrite, causing the mixed nitrate solution to be applied in the form of drops or droplets to a surface that is heated to a temperature above the decomposition point of the most stable nitrate present in the solution so that each drop or droplet becomes decomposed to form an intimate mixture of oxide powders of the calculated composition, said mixture generally containing some proportion of spinelstructure ferrites, without giving the more stable nitrates present in the solution a chance of becoming separated from the less stable nitrates, removing the resulting mixed powder at the rate at which it is formed, and subjecting the removed mixed powder to further heat treatment to convert more of the powder into spinel or magnetoplumbite or related structure, as the case may be, up to such percentage as to form a ferrite powder which after moulding and sintering will give a body having desired magnetic properties.

Preferably the nitrates of the individual metals are formed by dissolving each of the metals in question, or a suitable compound or mixture of compounds of such metal, in nitric acid, and the vapors formed as a result of this dissolving step and of the nitrate decomposition step being, together with the developed steam and added air or oxygen, employed for reconstitution of nitric acid which is then reintroduced into the process.

In the reconstitution of nitric acid from the decomposition gases it is necessary, in order to avoid health risks, to remove nitrous gases from the exhaust down to a low percentage, and while this hitherto required the provision of a relatively high number of absorption columns, this number can, according to a feature of the invention, be considerably reduced in the case of the manufacture of ferrites containing a metal having a basic oxide, more particularly zinc or barium, by supplying that metal in the form of its basic oxide, and causing the tail gases of the absorption system to pass through a dispersion of this oxide, preferably bubbling it through a dispersion in water, the dispersion being converted to the corresponding nitrate or nitrite, the solution then being used in the manufacture of the ferrite powder.

The method of the invention is applicable to all metals used in ferrites known to us and is inexpensive in view of the fact that the nitric acid introduced into the process is substantially all recovered for further use, and that, apart from the generally lower price of each metal compared with that of its oxide of comparable purity, iron, which forms the main constituent of many ferrites, can be employed in the form of scrap stampings, which are available to a specification at a very low price.

In order that the invention may be more easily understood, one method of manufacturing ferrite powder for manganese zinc ferrite Mn Zn (Fe o will now be described by way of example.

EXAMPLE The starting materials of the process comprise manganese metallic iron in the fonn of mild-steel scrap stampings sold to specification and zinc in the form of metal or, preferably, of zinc oxide, and sufficient nitric acid for their conversion to nitrates.

The manganese metal, the iron, and the zinc, the latter preferably wholly or partly as an aqueous dispersion of zinc oxide after its use in the absorption of NO from the tail gases of the nitric-acid recovery system described further below, are individually brought to solution in nitric acid to obtain nitrate solutions of known concentration. These solutions are then mixed in such proportions that the individual metals are present in the mixed nitrate solution in the desired proportions. This mixed solution is drop-fed or preferably spray-fed into a reactor to strike a surface maintained at a temperature of about 250 C. il0 which is slightly above the decomposition temperature of the most stable one of the nitrates employed, and the area of heated surface in contact with the incoming nitrate solution is arranged to be sufficient to ensure decomposition of the nitrate without allowing any liquid to accumulate. This surface may be, at least partially, constituted by some of the granular decomposition product for example as described in our copending Great Britain application No. 3,456,5/67. Thus an intimately mixed oxide powder containing some ferrite of spinel structure is obtained. The reactor is so constructed as to automatically discharge the powder and feed it into a heated calcination chamber, which is maintained at a temperature of 800 C. for a period of 17 minutes. This calcining treatment could if desired be carried out at some other temperature above 650 C. with corresponding adjustment of the period, but 800 is at present considered to be the most desirable temperature. This calcination chamber is fitted with a screw conveyor or other conveying means so operated as to maintain the mixture at this temperature for the time required for the powder leaving the calcination chamber to obtain the desired ferrite content to be suitable for final sintering after shaping; which in the specific example was a ferrite powder with 60 spinel structure and having the following composition in which percent as determined by chemical analysis viz: R1 0, 71.0, ZnO 14.02, MnO 15.06.

The nitrous fumes, together with steam formed during the operation and the fumes from the solution stages are then led together with an excess of air or oxygen, to a nitric-acid recovery system, and the recovered nitric acid is reused at the dissolving stage of the process. In the preferred form of the process, in which zinc oxide forms one of the starting materials, the tail gases of the recovery process are bubbled through an aqueous suspension of the zinc oxide to remove residual NO by conversion to Zn (N0 and Zn (N0 such conversion may take place according to the formula 2Zn0+4 NO+20 Zn( NO +Zn( N0 The resulting substances can replace the zinc or zinc oxide in the formation of zinc nitrate by treatment with nitric acid.

The accompanying drawing is a fiow sheet of the example described.

The raw materials, viz: iron scrap, manganese metal, and zinc oxide are supplied from three containers 1, 2, and 3 respectively. The metallic iron and manganese are each subjected to treatment with a solution of nitric acid, as indicated at 4 and thus converted respectively into an iron nitrate solution, stored in a reservoir 5, and a manganese nitrate solution, stored in a second reservoir 6. The zinc oxide from container 3 is eventually used to similarly produce a solution of zinc nitrate stored in a container 7, but before being subjected to the nitric-acid treatment of stage 4, it is first used for removal, in the first stage or stages of a nitric-acid recuperation system 12, of the residue of nitrous and nitric oxides from the nitration stage 4 and from a calcining stage 9 to be referred to further below.

The solution of iron nitrate, manganese nitrate, and zinc nitrate from reservoirs 5, 6 and 7 respectively are fed in the molecular proportions corresponding to the composition of the ferrite powder required to be produced, in a mixing stage 8 where, due to thepresence of each component in an aqueous solution, a very uniform distribution is achieved, and the mixed solution is sprayed in a hot reactor 9 in the presence of air on to a surface heated to 250 C., which is somewhat above the decomposition temperature of the nitrate having the highest decomposition temperature of the three nitrates. Decomposition of the nitrates and evaporation of the solvent water are arranged to take place so rapidly that there is practically no chance of any unmixing. As a result a very uniform solid-oxide mixture, partly already in compound spinel structure, and having a quantitative composition corresponding to that of the ferrite powder to be produced is formed in granular form. This mixture is transferred in a continuous flow to a calcining stage 10, where at 800 C. the mutual reaction of the oxides is continued to the extent necessary for the material to leave this stage, after 17 minutes to be delivered at 11 in the form of a ferrite powder with 60 percent spinel structure and containing 71.0 percent by weight of Fe O l4.02-percent by weight of ZnO and 15.06 percent by weight of MnO.

It will be readily appreciated by those skilled in the art that the process described by way of example requires modification if ferrites other than manganese-zinc ferrites are to be formed. Thus for example when it is required to form bariumstrontium ferrite (Ba, Sr) Fe,,o,,, the reaction temperature for the decomposition should be preferably at least approximately 750 C,

The process according to the invention, more particularly in its preferred form, offers quite a number of advantages over various existing processes for the manufacture of ferrite powder. Thus the powder produced is reproducible with respect to composition, specific surface, and reactivity. The process is continuous and is controllable inasmuch as the solutions are perfectly miscible and in each solution a sample is consistently representative of the bulk. For similar reasons continuous analysis is possible. Furthermore the process is cheap: In the case of the specific example, the main constituent, viz: iron, is obtainable at a standard specification at a April 1967 price of approximately l2per ton whereas in April 1967 iron oxide of similar purity costs to90 per ton. In contrast to the case of coprecipitation, no filtration or decantation is required, and the produce is delivered as a freeflowing powder. Furthermore the process of the invention is suitable for continuous operation, and it is applicable to all ferrites at present in commercial use because all nitrates are water-soluble and all are decomposable. by heat. The only chemical reactant involved, namely nitric acid, is recirculated, thus minimizing the cost of treatment chemicals, and finally the ferrites obtained are closely reproducible because there is less variation in the purity of the raw materials employed compared with the oxides which are used in the most commonly used ceramic process. 1

What is claimed is:

l. A continuous process for the production of a ferrite material in which at least one of the constituent metals has a basic oxide, comprising the steps of forming a nitrate solution of each metal contained in the ferrite by dissolving in nitric acid a material of the group consisting of the metal and compounds of the metal, mixing said nitrate solutions In accordance with the required molecular quantities of each metal, heating the resulting mixed aqueous solution to effect evaporation of the water and heat-decomposition of the.

nitrates so as to produce an oxide mixture having a desired ferrite content, passing the vapors produced by the forming of said nitrate solution of each metal and the vapors produced by the heating and decomposition of the mixed aqueous solution through an absorption system to reconstitute nitric acid, providing an aqueous dispersion of a basic oxide of such constituent metal, passing the tail gases of the absorption system through said aqueous dispersion to convert at least one of the basic oxide in said aqueous dispersion to a nitrogen compound of the group comprising nitrates and nitrites of said constituent metal, mixing the thus converted dispersion with part of the nitric acid reconstituted by the absorption system to form at least part of the nitrate solution of said constituent metal employed in said mixing step, and mixing the remainder of said reconstituted nitric acid with the materials respectively comprising the remainder of said metals and compounds of said metals so that in continuous operation substantially the whole of the nitrates solutions employed in the process are gained by recirculation of the reconstituted nitric acid and the use of said tail gases.

2. A process as claimed in claim 1, wherein the metal supplied in the form of a basic oxide is a metal of the group constituted by zinc and barium.

3. A method as claimed in claim 1, wherein all said constituent metal is provided in the form of such basic oxide, and all this basic oxide is utilized to form said aqueous suspension. 

2. A process as claimed in claim 1, wherein the metal supplied in the form of a basic oxide is a metal of the group constituted by zinc and barium.
 3. A method as claimed in claim 1, wherein all said constituent metal is provided in the form of such basic oxide, and all this basic oxide is utilized to form said aqueous suspeNsion. 